abnormal st segment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An electrocardiographic anomaly of the ST segment, which is the segment that connects the QRS complex and the T wave. The ST segment normally has a duration of 80 to 120 ms, is flat and at the same level (isoelectric) as the PR and TP segment. (Human Phenotype Ontology, HP_0012249)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012249
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Genes

4 genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3
SCN1B sodium channel, voltage gated, type I beta subunit
SCN3B sodium channel, voltage gated, type III beta subunit